510(k) K234060

KIDNEYvault Portable Renal Perfusion System by Paragonix Technologies — Product Code KDN

K234060 is an FDA 510(k) premarket notification submitted by Paragonix Technologies for the device "KIDNEYvault Portable Renal Perfusion System". The FDA issued a decision of Substantially Equivalent on October 23, 2024. The device falls under product code KDN (System, Perfusion, Kidney), a Class II device regulated under 21 CFR 876.5880. Paragonix Technologies has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 23, 2024
Date Received
December 22, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Perfusion, Kidney
Device Class
Class II
Regulation Number
876.5880
Review Panel
GU
Submission Type